Procter & Gamble Mfg. Co.

Procter & Gamble Mfg. Co. — FDA 510(k) Submissions

Procter & Gamble Mfg. Co. has submitted 72 FDA 510(k) premarket notifications since 1976, of which 72 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Drape, Surgical, Pad, Menstrual, Unscented, Pad, Menstrual, Scented, Scented-deodorized, Garment, Protective, For Incontinence, Gown, Surgical . Use the specialty filter in the sidebar to narrow results.